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ELISA GINTER, D.O.
D.O.
Family Medicine Physician
NPI: 1871650507IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
OS 6732(FL)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
MICHIGAN STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE
Class of 1986
Research & Publications (20)
[Genetic epidemiological study of Bashkortostan Republic: the diversity of monogenic hereditary diseases in five districts].
PMID 19534428·Genetika·2009
8-other
Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.
PMID 19172990·Eur J Hum Genet·2009
8-other
Alcoholism: recent advances in epidemiology, biochemistry and genetics.
PMID 19507669·Bratisl Lek Listy·2009
6-review
[Genetic epidemiological study of Bashkortostan Republic: the effect of genetic structure of population on the load of monogenic hereditary diseases].
PMID 19507708·Genetika·2009
8-other
Adult obesity at the beginning of the 21st century: epidemiology, pathophysiology and health risk.
PMID 18630807·Bratisl Lek Listy·2008
6-review
Ethanol and cardiovascular diseases: epidemiological, biochemical and clinical aspects.
PMID 19348387·Bratisl Lek Listy·2008
6-review
[Prevalences of hereditary diseases in various populations in Russia].
PMID 17990523·Genetika·2007
8-other
Chronic vitamin C deficiency increases the risk of cardiovascular diseases.
PMID 18225482·Bratisl Lek Listy·2007
6-review
High incidence of mutations in BRCA1 and BRCA2 genes in ovarian cancer.
PMID 18256760·Bull Exp Biol Med·2007
8-other
The prevalence of female obesity in the world and in the Slovak Gypsy women.
PMID 17694806·Bratisl Lek Listy·2007
8-other
Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state.
PMID 17564961·Am J Hum Genet·2007
7-preclinical
[Population study of the Udmurt population: analysis of ten polymorphic DNA loci of the nuclear genome].
PMID 17633563·Genetika·2007
8-other
[Analysis of polymorphism at nine nuclear genome DNA loci in maris].
PMID 16583710·Genetika·2006
8-other
Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.
PMID 17095700·Science·2006
8-other
New mutations in the APC gene in familial adenomatous polyposis: detection, characterization, and analysis.
PMID 16027851·Bull Exp Biol Med·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2929 N UNIVERSITY DR STE 104
CORAL SPRINGS, FL 33065 - Phone
- (954) 289-4777
Quick Facts
- NPI
- 1871650507
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 40
- Publications
- 20
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